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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
Description: cGMP procedures , Self - Inspection (Internal Quality Audit) , Quality Assurance SOPs and Review of other department Sops, Review of Tech transfer, process validation protocols, MFR/ BMR and Executed batch records, production deviations, Sampling of in - process, reserve samples, stability samples of drug substance , Review of MFR, BMR, IOQ Protocols, cleaning validation and Report. Experience Required: 8 - 10 YearsLocation: HyderabadDepartment: Quality AssuranceUnit: Salary: At par within industry,
Keyskills :
techtransferqualityassuranceprocessvalidationcleaningvalidationbmrmfrcgmprecsamplingassuranceprotocolsvalidationinspectiondeviationsBatchReleaseCAPAsBatchControlEBRatchrecQualityIn